MeSH Browser

MeSH Supplementary: Protoporphyria, Erythropoietic, X-Linked Dominant
Unique ID: C567464
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567464
Entry Term(s): Erythrohepatic Protoporphyria, X-Linked; Xldpt
Registry Numbers: 0
Heading Mapped to: 5-Aminolevulinate Synthetase / deficiency; *Genetic Diseases, X-Linked; *Protoporphyria, Erythropoietic
Frequency: 13
Note: mutation in ALAS2
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Protoporphyria, Erythropoietic, X-Linked Dominant MeSH Supplementary Concept Data 2025